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Niloofar Bazazzadegan, Abraham M. Sheffield, Masoomeh Sobhani, Kimia Kahrizi, Nicole C. Meyer, Guy Van Camp, Nele Hilgert, Seyedeh Sedigheh Abedini, Farkhondeh Habibi, Ahmad Daneshi, Carla Nishimura, Matthew R. Avenarius, Mohammad Farhadi, Richard J.H. Smith and Hossein Najmabadi Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss American Journal of Medical Genetics Part A 155

Article first published online: 11 APR 2011 | DOI: 10.1002/ajmg.a.33209

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